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Damage-induced neuronal endopeptidase (DINE) is a unique metallopeptidase expressed in response to neuronal damage and activates superoxide scavengers

机译:损伤诱导神经元内肽酶(DINE)是一种独特的金属肽酶,可响应神经元损伤而表达并激活超氧化物清除剂

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摘要

We isolated a membrane-bound metallopeptidase, DINE (damage-induced neuronal endopeptidase), by differential display PCR using rat normal and axotomized hypoglossal nuclei. The most marked properties of DINE were neuron-specific expression and a striking response to axonal injury in both the central nervous system and peripheral nervous system. For instance, cranial and spinal nerve transection, ischemia, corpus callosum transection, and colchicine treatment increased DINE mRNA expression in the injured neurons, whereas kainate-induced hyperexcitation, immobilization, and osmotic stress failed to up-regulate DINE mRNA. Expression of DINE in COS cells partially inhibited C2-ceramide-induced apoptosis, probably because of the activation of antioxidant enzymes such as Cu/Zn-superoxide dismutase, Mn-superoxide dismutase, and glutathione peroxidase through the proteolytic activity of DINE. These data provide insight into the mechanism of how injured neurons protect themselves against neuronal death.
机译:我们使用大鼠正常和轴突化的舌下核,通过差异展示PCR分离了一种膜结合的金属肽酶DINE(损伤诱导的神经元内肽酶)。 DINE的最显着特性是神经元特异性表达和中枢神经系统和周围神经系统对轴突损伤的惊人反应。例如,颅神经和脊髓神经横切,局部缺血,call体横切和秋水仙碱治疗增加了受损神经元中DINE mRNA的表达,而海藻酸盐诱导的过度兴奋,固定和渗透压未能上调DINE mRNA。 DINE在COS细胞中的表达部分抑制了C2-神经酰胺诱导的细胞凋亡,这可能是由于DINE的蛋白水解活性激活了抗氧化酶,例如Cu / Zn超氧化物歧化酶,Mn超氧化物歧化酶和谷胱甘肽过氧化物酶。这些数据提供了有关受损神经元如何保护自己免受神经元死亡的机制的见解。

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